Textor Jamie A, Norris Jeffrey W, Tablin Fern
Department of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California-Davis, Davis, CA 95616, USA.
Am J Vet Res. 2011 Feb;72(2):271-8. doi: 10.2460/ajvr.72.2.271.
To test the hypotheses that preparation method, exposure to shear force, and exposure to collagen affect the release of growth factors from equine platelet-rich plasma (PRP).
PRP obtained from 6 horses.
PRP was prepared via 2 preparation methods (tube and automated) and subjected to 6 treatment conditions (resting, detergent, exposure to shear via 21- and 25-gauge needles, and exposure to collagen [10 and 20 μg/mL]). Concentrations of platelet-derived growth factor, isoform BB (PDGF-BB); transforming growth factor β, isoform 1 (TGFβ₁); and insulin-like growth factor, isoform 1 (IGF-1) were quantified by use of ELISAs. Statistical analysis was conducted via repeated-measures ANOVA.
Platelet numbers were significantly higher in tube-prepared PRP than in automated-prepared PRP Growth factor concentrations did not differ significantly between preparation methods. Mean PDGF-BB concentration ranged from 134 to 7,157 pg/mL, mean TGFβ₁ concentration ranged from 1,153 to 22,677 pg/mL, and mean IGF-1 concentration ranged from 150 to 280 ng/mL. Shear force did not affect growth factor concentrations. Dose-dependent increases in PDGF-BB and TGFβ₁ were detected in response to collagen, but equalled only 10% of the estimated total platelet content. Concentrations of IGF-1 were not significantly different among treatments and negative or positive control treatments. Serum concentrations of PDGF-BB and TGFβ₁ exceeded concentrations in PRP for most treatment conditions.
Release of growth factors from equine PRP was negligible as a result of the injection process alone. Investigation of platelet-activation protocols is warranted to potentially enhance PRP treatment efficacy in horses.
检验以下假设,即制备方法、剪切力作用及胶原蛋白接触会影响马富血小板血浆(PRP)中生长因子的释放。
从6匹马获取的PRP。
通过2种制备方法(试管法和自动化法)制备PRP,并使其接受6种处理条件(静置、去污剂处理、通过21号和25号针头施加剪切力、接触胶原蛋白[10和20μg/mL])。采用酶联免疫吸附测定法(ELISA)对血小板衍生生长因子BB异构体(PDGF-BB)、转化生长因子β1异构体(TGFβ₁)和胰岛素样生长因子1异构体(IGF-1)的浓度进行定量。通过重复测量方差分析进行统计分析。
试管法制备的PRP中的血小板数量显著高于自动化法制备的PRP。两种制备方法之间生长因子浓度无显著差异。PDGF-BB平均浓度范围为134至7157 pg/mL,TGFβ₁平均浓度范围为1153至22677 pg/mL,IGF-1平均浓度范围为150至280 ng/mL。剪切力不影响生长因子浓度。检测到胶原蛋白作用下PDGF-BB和TGFβ₁呈剂量依赖性增加,但仅相当于估计总血小板含量的10%。各处理组与阴性或阳性对照组之间IGF-1浓度无显著差异。在大多数处理条件下,血清中PDGF-BB和TGFβ₁的浓度超过PRP中的浓度。
仅注射过程导致马PRP中生长因子的释放可忽略不计。有必要研究血小板激活方案,以潜在提高马PRP治疗效果。